American Society of Hirudotherapy

Argatroban anticoagulation in renal dysfunction: a literature analysis

Systematic review published in Nephron. Clinical practice (2008)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Meta-analysisClinical TrialsSafety & Infection ControlSalivary PharmacologyHursting MJ et al. · Nephron. Clinical practice, 2008

Abstract

BACKGROUND/AIMS: Argatroban, a hepatically metabolized direct thrombin inhibitor, is approved for use in heparin-induced thrombocytopenia (HIT; several countries) and in antithrombin-deficient patients undergoing hemodialysis (Japan). This literature analysis aimed to determine the effects of renal function on argatroban pharmacokinetics, pharmacodynamics, and its therapeutic dose in HIT and to evaluate argatroban dosing and safety during renal replacement therapy (RRT) and in adults with renal dysfunction undergoing surgical or invasive procedures. METHODS: A literature search identified 34 publications (12 prospective studies, 4 retrospective studies, 18 anecdotal reports) that together described 644 argatroban-treated patients (446 with HIT, 82 with antithrombin deficiency) with varying degrees of renal function. Pertinent data were extracted and summarized. RESULTS: In pharmacokinetic studies (40 patients, overall), renal dysfunction exerted little or no clinically significant effects on argatroban pharmacokinetic parameters. For argatroban therapy in HIT, evidence existed that an initial 2 microg/kg/min dose was sometimes excessive; patients with hepatic dysfunction, irrespective of renal function, required reduced initial doses; lesser doses were required in combined hepatic and renal dysfunction than hepatic dysfunction, and for each 30 ml/min decrease in patient creatinine clearance, the therapeutic dose decreased approximately 0.1-0.6 microg/kg/min. Argatroban was well tolerated and enabled RRT with little or no thrombotic or hemorrhagic complications. Experiences with argatroban in renally impaired patients undergoing procedures besides RRT were limited. CONCLUSION: Current literature suggests that argatroban is well tolerated and provides adequate anticoagulation in patients with renal dysfunction or failure, including individuals with HIT or antithrombin deficiency where anticoagulant options are limited.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleMeta-Analysis
Indexed MeSH termsAnticoagulantsArginineComorbidityHumansPipecolic AcidsPrevalenceRenal InsufficiencySulfonamidesThrombosisTreatment Outcome

Summary

Argatroban, a hepatically metabolized direct thrombin inhibitor, is approved for use in heparin-induced thrombocytopenia (HIT; several countries) and in antithrombin-deficient patients undergoing hemodialysis (Japan).

Why This Matters for Hirudotherapy

This literature analysis of 34 publications examined argatroban pharmacokinetics, pharmacodynamics, dosing, and safety across 644 argatroban-treated patients with varying degrees of renal function, including those undergoing renal replacement therapy. The authors conclude that argatroban is well tolerated and provides adequate anticoagulation in patients with renal dysfunction, though reduced initial doses may be needed when hepatic dysfunction coexists, and therapeutic doses decrease with declining creatinine clearance. The abstract describes argatroban as a hepatically metabolized direct thrombin inhibitor but makes no mention of hirudin, leeches, or any leech-derived compounds. No defensible connection to hirudotherapy or the leech secretome is evident from this abstract.

Citation

Argatroban anticoagulation in renal dysfunction: a literature analysis

Hursting MJ et al. · Nephron. Clinical practice, 2008

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